I want to calculate only intron reads in my RNA sequencing. So I generate a GTF file which only contain intron site information. Then save it as gtf.
In linux, I use featurecounts like:
featureCounts -T 8 -p
-t intron -g gene_name
-a intron.gtf -o intron.txt
*.sam
Then it shows:
ERROR: no features were loaded in format GTF. The annotation format can be specified by the '-F' option, and the required feature type can be specified by the '-t' option..
I think my GTF has wrong format. So how can I solve it?